Improved oxygenation promotes CFTR maturation and trafficking in MDCK monolayers

Am J Physiol Cell Physiol. 2001 Jan;280(1):C135-45. doi: 10.1152/ajpcell.2001.280.1.C135.

Abstract

Culturing airway epithelial cells with most of the apical media removed (air-liquid interface) has been shown to enhance cystic fibrosis transmembrane conductance regulator (CFTR)-mediated Cl(-) secretory current. Thus we hypothesized that cellular oxygenation may modulate CFTR expression. We tested this notion using type I Madin-Darby canine kidney cells that endogenously express low levels of CFTR. Growing monolayers of these cells for 4 to 5 days with an air-liquid interface caused a 50-fold increase in forskolin-stimulated Cl(-) current, compared with conventional (submerged) controls. Assaying for possible changes in CFTR by immunoprecipitation and immunocytochemical localization revealed that CFTR appeared as an immature 140-kDa form intracellularly in conventional cultures. In contrast, monolayers grown with an air-liquid interface possessed more CFTR protein, accompanied by increases toward the mature 170-kDa form and apical membrane staining. Culturing submerged monolayers with 95% O(2) produced similar improvements in Cl(-) current and CFTR protein as air-liquid interface culture, while increasing PO(2) from 2.5% to 20% in air-liquid interface cultures yielded graded enhancements. Together, our data indicate that improved cellular oxygenation can increase endogenous CFTR maturation and/or trafficking.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Culture Techniques / methods
  • Cell Differentiation / drug effects*
  • Cell Differentiation / physiology
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cell Polarity / drug effects
  • Cell Polarity / physiology
  • Cells, Cultured / cytology
  • Cells, Cultured / drug effects
  • Cells, Cultured / metabolism*
  • Colforsin / metabolism
  • Colforsin / pharmacology
  • Culture Media / pharmacology
  • Cystic Fibrosis / metabolism
  • Cystic Fibrosis / pathology
  • Cystic Fibrosis / physiopathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism*
  • Dogs
  • Hypoxia / metabolism
  • Hypoxia / pathology
  • Hypoxia / physiopathology
  • Oxygen / pharmacology*
  • Protein Transport / physiology*
  • RNA, Messenger / metabolism

Substances

  • Culture Media
  • RNA, Messenger
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Colforsin
  • Oxygen